References analysis of the Wikipedia article "Turner syndrome" in the English version

doi.org

Donaldson MD, Gault EJ, Tan KW, Dunger DB (June 2006). "Optimising management in Turner syndrome: from infancy to adult transfer". Archives of Disease in Childhood. 91 (6): 513–520. doi:10.1136/adc.2003.035907. PMC 2082783. PMID 16714725. Archived from the original on 7 March 2012.

Sybert VP, McCauley E (September 2004). "Turner's syndrome". The New England Journal of Medicine. 351 (12): 1227–1238. doi:10.1056/NEJMra030360. PMID 15371580.

Knoll MM, Strickland J, Jacobson JD (2022). "Can Boys Have Turner Syndrome? More than a Question of Semantics". Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation. 16 (1): 19–26. doi:10.1159/000518092. PMID 34515231.

Lin AE, Prakash SK, Andersen NH, Viuff MH, Levitsky LL, Rivera-Davila M, et al. (October 2019). "Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years". American Journal of Medical Genetics. Part A. 179 (10): 1987–2033. doi:10.1002/ajmg.a.61310. PMID 31418527.

Gunther DF, Eugster E, Zagar AJ, Bryant CG, Davenport ML, Quigley CA (September 2004). "Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life". Pediatrics. 114 (3): 640–644. doi:10.1542/peds.2003-1122-L. PMID 15342833. S2CID 22596252.

Tuke MA, Ruth KS, Wood AR, Beaumont RN, Tyrrell J, Jones SE, et al. (April 2019). "Mosaic Turner syndrome shows reduced penetrance in an adult population study". Genetics in Medicine. 21 (4): 877–886. doi:10.1038/s41436-018-0271-6. PMC 6752315. PMID 30181606.

Bertapelli F, Barros-Filho A, Antonio MÂ, Barbeta CJ, de Lemos-Marini SH, Guerra-Junior G (2014). "Growth curves for girls with Turner syndrome". BioMed Research International. 2014 (1): 687978. doi:10.1155/2014/687978. PMC 4052048. PMID 24949463.

Oliveira CS, Alves C (October 2011). "The role of the SHOX gene in the pathophysiology of Turner syndrome". Endocrinologia y Nutricion. 58 (8): 433–442. doi:10.1016/j.endoen.2011.06.003. PMID 21925981.

Li P, Cheng F, Xiu L (April 2018). "Height outcome of the recombinant human growth hormone treatment in Turner syndrome: a meta-analysis". Endocrine Connections. 7 (4): 573–583. doi:10.1530/EC-18-0115. PMC 5900457. PMID 29581156.

Sheanon NM, Backeljauw PF (26 August 2015). "Effect of oxandrolone therapy on adult height in Turner syndrome patients treated with growth hormone: a meta-analysis". International Journal of Pediatric Endocrinology. 2015 (1): 18. doi:10.1186/s13633-015-0013-3. PMC 4551522. PMID 26322078.

Cui X, Cui Y, Shi L, Luan J, Zhou X, Han J (November 2018). "A basic understanding of Turner syndrome: Incidence, complications, diagnosis, and treatment". Intractable & Rare Diseases Research. 7 (4): 223–228. doi:10.5582/irdr.2017.01056. PMC 6290843. PMID 30560013.

Atton G, Gordon K, Brice G, Keeley V, Riches K, Ostergaard P, et al. (December 2015). "The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review". European Journal of Human Genetics. 23 (12): 1634–1639. doi:10.1038/ejhg.2015.41. PMC 4486366. PMID 25804399.

Lowenstein EJ, Kim KH, Glick SA (May 2004). "Turner's syndrome in dermatology". Journal of the American Academy of Dermatology. 50 (5): 767–776. doi:10.1016/j.jaad.2003.07.031. PMID 15097963.

Miguel-Neto J, Carvalho AB, Marques-de-Faria AP, Guerra-Júnior G, Maciel-Guerra AT (April 2016). "New approach to phenotypic variability and karyotype-phenotype correlation in Turner syndrome". Journal of Pediatric Endocrinology & Metabolism. 29 (4): 475–479. doi:10.1515/jpem-2015-0346. PMID 26812779. S2CID 43332484.

Davenport ML (April 2010). "Approach to the patient with Turner syndrome". The Journal of Clinical Endocrinology and Metabolism. 95 (4): 1487–1495. doi:10.1210/jc.2009-0926. PMID 20375216.

Reed T (1981). "Dermatoglyphics in medicine--problems and use in suspected chromosome abnormalities". American Journal of Medical Genetics. 8 (4): 411–429. doi:10.1002/ajmg.1320080407. PMID 7018239.

Turtle EJ, Sule AA, Webb DJ, Bath LE (July 2015). "Aortic dissection in children and adolescents with Turner syndrome: risk factors and management recommendations". Archives of Disease in Childhood. 100 (7): 662–666. doi:10.1136/archdischild-2014-307080. PMID 25573747. S2CID 206857477.

Gravholt CH, Viuff MH, Brun S, Stochholm K, Andersen NH (October 2019). "Turner syndrome: mechanisms and management". Nature Reviews. Endocrinology. 15 (10): 601–614. doi:10.1038/s41574-019-0224-4. PMID 31213699. S2CID 190653543.

Roulot D (January 2013). "Liver involvement in Turner syndrome". Liver International. 33 (1): 24–30. doi:10.1111/liv.12007. PMID 23121401.

Fanos V, Schena S, Dal Moro A, Portuese A, Antoniazzi F (August 2000). "Multicystic kidney dysplasia and Turner syndrome: two cases and a literature review". Pediatric Nephrology. 14 (8–9): 754–757. doi:10.1007/PL00013430. PMID 10955920. S2CID 42881441.

Morin JP, Saltzman AF (August 2021). "Gonadoblastoma in Turner Syndrome: A Surprise in a Streak". Urology. 154: 278–280. doi:10.1016/j.urology.2021.02.050. PMID 33961893. S2CID 233997606.

Dabrowski E, Johnson EK, Patel V, Hsu Y, Davis S, Goetsch AL, et al. (February 2020). "Turner Syndrome with Y Chromosome: Spontaneous Thelarche, Menarche, and Risk of Malignancy". Journal of Pediatric and Adolescent Gynecology. 33 (1): 10–14. doi:10.1016/j.jpag.2019.08.011. PMC 7413626. PMID 31465855.

Chen J, Guo M, Luo M, Deng S, Tian Q (August 2021). "Clinical characteristics and management of Turner patients with a small supernumerary marker chromosome". Gynecological Endocrinology. 37 (8): 730–734. doi:10.1080/09513590.2021.1911992. PMID 33870841. S2CID 233298107.

Barros BA, Moraes SG, Coeli FB, Assumpção JG, De Mello MP, Maciel-Guerra AT, et al. (December 2011). "OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences". Human Reproduction. 26 (12): 3450–3455. doi:10.1093/humrep/der310. PMID 21930534.

Röthlisberger B, Zerova T, Kotzot D, Buzhievskaya TI, Balmer D, Schinzel A (December 2001). "Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child". Journal of Medical Genetics. 38 (12): 885–888. doi:10.1136/jmg.38.12.885. PMC 1734780. PMID 11768396.

Bonnard Å, Bark R, Hederstierna C (March 2019). "Clinical update on sensorineural hearing loss in Turner syndrome and the X-chromosome". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 181 (1): 18–24. doi:10.1002/ajmg.c.31673. PMID 30632288. S2CID 58589784.

Álvarez-Nava F, Racines-Orbe M, Witt J, Guarderas J, Vicuña Y, Estévez M, et al. (13 January 2020). "Metabolic Syndrome as a Risk Factor for Sensorineural Hearing Loss in Adult Patients with Turner Syndrome". The Application of Clinical Genetics. 13 (13): 25–35. doi:10.2147/TACG.S229828. PMC 6971290. PMID 32021381.

Denniston AK, Butler L (July 2004). "Ophthalmic features of Turner's syndrome". Eye. 18 (7): 680–684. doi:10.1038/sj.eye.6701323. PMID 15002027. S2CID 7567847.

Aversa T, Gallizzi R, Salzano G, Zirilli G, De Luca F, Valenzise M (January 2018). "Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome". Italian Journal of Pediatrics. 44 (1): 12. doi:10.1186/s13052-018-0447-3. PMC 5773039. PMID 29343299.

Dabrowski E, Jensen R, Johnson EK, Habiby RL, Brickman WJ, Finlayson C (2019). "Turner Syndrome Systematic Review: Spontaneous Thelarche and Menarche Stratified by Karyotype". Hormone Research in Paediatrics. 92 (3): 143–149. doi:10.1159/000502902. PMID 31918426. S2CID 210131881.

Journal of Pediatric and Adolescent Gynecology (October 2016). "Fertility Preservation in Women with Turner Syndrome: A Comprehensive Review and Practical Guidelines". Journal of Pediatric and Adolescent Gynecology. 29 (5): 409–416. doi:10.1016/j.jpag.2015.10.011. PMC 5015771. PMID 26485320.

Practice Committee of the American Society for Reproductive Medicine (February 2012). "Increased maternal cardiovascular mortality associated with pregnancy in women with Turner syndrome". Fertility and Sterility. 97 (2): 282–284. doi:10.1016/j.fertnstert.2011.11.049 (inactive 31 January 2024). PMID 22192347.{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)

Elsheikh M, Dunger DB, Conway GS, Wass JA (February 2002). "Turner's syndrome in adulthood". Endocrine Reviews. 23 (1): 120–140. doi:10.1210/edrv.23.1.0457. PMID 11844747.

Gravholt CH, Fedder J, Naeraa RW, Müller J (September 2000). "Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: a population study". The Journal of Clinical Endocrinology and Metabolism. 85 (9): 3199–3202. doi:10.1210/jcem.85.9.6800. PMID 10999808.

Mazzocco MM (October 2006). "The cognitive phenotype of Turner syndrome: Specific learning disabilities". International Congress Series. 1298: 83–92. doi:10.1016/j.ics.2006.06.016. PMC 2742423. PMID 19750135.

Berkovitz G, Stamberg J, Plotnick LP, Lanes R (June 1983). "Turner syndrome patients with a ring X chromosome". Clinical Genetics. 23 (6): 447–453. doi:10.1111/j.1399-0004.1983.tb01980.x. PMID 6883789. S2CID 13544594.

McCauley E, Feuillan P, Kushner H, Ross JL (December 2001). "Psychosocial development in adolescents with Turner syndrome". Journal of Developmental and Behavioral Pediatrics. 22 (6): 360–365. doi:10.1097/00004703-200112000-00003. PMID 11773800. S2CID 39749059.

Christopoulos P, Deligeoroglou E, Laggari V, Christogiorgos S, Creatsas G (March 2008). "Psychological and behavioural aspects of patients with Turner syndrome from childhood to adulthood: a review of the clinical literature". Journal of Psychosomatic Obstetrics and Gynaecology. 29 (1): 45–51. doi:10.1080/01674820701577078. PMID 17852655. S2CID 8149629.

Reimann GE, Bernad Perman MM, Ho PS, Parks RA, Comis LE (August 2018). "Psychosocial Characteristics of Women with a Delayed Diagnosis of Turner Syndrome". The Journal of Pediatrics. 199: 206–211. doi:10.1016/j.jpeds.2018.03.058. PMC 6063780. PMID 29753544.

Gravholt CH, Juul S, Naeraa RW, Hansen J (January 1996). "Prenatal and postnatal prevalence of Turner's syndrome: a registry study". BMJ. 312 (7022): 16–21. doi:10.1136/bmj.312.7022.16. PMC 2349728. PMID 8555850.

Crespi B (August 2008). "Turner syndrome and the evolution of human sexual dimorphism". Evolutionary Applications. 1 (3): 449–461. Bibcode:2008EvApp...1..449C. doi:10.1111/j.1752-4571.2008.00017.x. PMC 3352375. PMID 25567727.

Wang H, Wang T, Yang N, He Y, Chen L, Hong L, et al. (June 2017). "The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype". Oncology Letters. 13 (6): 4385–4389. doi:10.3892/ol.2017.5965. PMC 5452876. PMID 28588710.

Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.

Monroy N, López M, Cervantes A, García-Cruz D, Zafra G, Canún S, et al. (January 2002). "Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes". American Journal of Medical Genetics. 107 (3): 181–189. doi:10.1002/ajmg.10113. PMID 11807897.

Uematsu A, Yorifuji T, Muroi J, Kawai M, Mamada M, Kaji M, et al. (August 2002). "Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype". American Journal of Medical Genetics. 111 (2): 134–139. doi:10.1002/ajmg.10506. PMID 12210339.

Frías JL, Davenport ML, et al. (Committee on Genetics Section on Endocrinology) (March 2003). "Health supervision for children with Turner syndrome". Pediatrics. 111 (3): 692–702. doi:10.1542/peds.111.3.692. PMID 12612263.

Saygin D, Tabib T, Bittar HE, Valenzi E, Sembrat J, Chan SY, et al. (2006). "Transcriptional profiling of lung cell populations in idiopathic pulmonary arterial hypertension". Pulmonary Circulation. 10 (1): 26–29. doi:10.1016/j.ics.2006.07.005. PMC 7052475. PMID 32166015.

Stochholm K, Juul S, Juel K, Naeraa RW, Gravholt CH (October 2006). "Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome". The Journal of Clinical Endocrinology and Metabolism. 91 (10): 3897–3902. doi:10.1210/jc.2006-0558. PMID 16849410.

Bolar K, Hoffman AR, Maneatis T, Lippe B (February 2008). "Long-term safety of recombinant human growth hormone in turner syndrome". The Journal of Clinical Endocrinology and Metabolism. 93 (2): 344–351. doi:10.1210/jc.2007-1723. PMID 18000090.

Davenport ML, Crowe BJ, Travers SH, Rubin K, Ross JL, Fechner PY, et al. (September 2007). "Growth hormone treatment of early growth failure in toddlers with Turner syndrome: a randomized, controlled, multicenter trial". The Journal of Clinical Endocrinology and Metabolism. 92 (9): 3406–3416. doi:10.1210/jc.2006-2874. PMID 17595258.

Mohamed S, Alkofide H, Adi YA, Amer YS, AlFaleh K, et al. (Cochrane Metabolic and Endocrine Disorders Group) (October 2019). "Oxandrolone for growth hormone-treated girls aged up to 18 years with Turner syndrome". The Cochrane Database of Systematic Reviews. 2019 (10). doi:10.1002/14651858.CD010736.pub2. PMC 6820693. PMID 31684688.

Urbach A, Benvenisty N (2009). "Studying early lethality of 45,XO (Turner's syndrome) embryos using human embryonic stem cells". PLOS ONE. 4 (1): e4175. Bibcode:2009PLoSO...4.4175U. doi:10.1371/journal.pone.0004175. PMC 2613558. PMID 19137066.

Saygin D, Tabib T, Bittar HE, Valenzi E, Sembrat J, Chan SY, et al. (1938). "Transcriptional profiling of lung cell populations in idiopathic pulmonary arterial hypertension". Pulmonary Circulation. 10 (1): 566–574. doi:10.1210/endo-23-5-566. PMC 7052475. PMID 32166015.

Ford CE, Jones KW, Polani PE, De Almeida JC, Briggs JH (April 1959). "A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome)". Lancet. 1 (7075): 711–713. doi:10.1016/S0140-6736(59)91893-8. PMID 13642858.

Ford C (April 4, 1959). "A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome)". The Lancet. 273 (7075): 711–713. doi:10.1016/S0140-6736(59)91893-8. PMID 13642858 – via ScienceDirect.

nih.gov

pubmed.ncbi.nlm.nih.gov

Sybert VP, McCauley E (September 2004). "Turner's syndrome". The New England Journal of Medicine. 351 (12): 1227–1238. doi:10.1056/NEJMra030360. PMID 15371580.

Lowenstein EJ, Kim KH, Glick SA (May 2004). "Turner's syndrome in dermatology". Journal of the American Academy of Dermatology. 50 (5): 767–776. doi:10.1016/j.jaad.2003.07.031. PMID 15097963.

Davenport ML (April 2010). "Approach to the patient with Turner syndrome". The Journal of Clinical Endocrinology and Metabolism. 95 (4): 1487–1495. doi:10.1210/jc.2009-0926. PMID 20375216.

Roulot D (January 2013). "Liver involvement in Turner syndrome". Liver International. 33 (1): 24–30. doi:10.1111/liv.12007. PMID 23121401.

Morin JP, Saltzman AF (August 2021). "Gonadoblastoma in Turner Syndrome: A Surprise in a Streak". Urology. 154: 278–280. doi:10.1016/j.urology.2021.02.050. PMID 33961893. S2CID 233997606.

Denniston AK, Butler L (July 2004). "Ophthalmic features of Turner's syndrome". Eye. 18 (7): 680–684. doi:10.1038/sj.eye.6701323. PMID 15002027. S2CID 7567847.

Elsheikh M, Dunger DB, Conway GS, Wass JA (February 2002). "Turner's syndrome in adulthood". Endocrine Reviews. 23 (1): 120–140. doi:10.1210/edrv.23.1.0457. PMID 11844747.

ncbi.nlm.nih.gov

nichd.nih.gov

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Morin JP, Saltzman AF (August 2021). "Gonadoblastoma in Turner Syndrome: A Surprise in a Streak". Urology. 154: 278–280. doi:10.1016/j.urology.2021.02.050. PMID 33961893. S2CID 233997606.

Denniston AK, Butler L (July 2004). "Ophthalmic features of Turner's syndrome". Eye. 18 (7): 680–684. doi:10.1038/sj.eye.6701323. PMID 15002027. S2CID 7567847.

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Turner syndrome (English Wikipedia)

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